FDA product code · General hospital

Water, Vascular Access Flush

Name: FDA decisions, review times, recalls and adverse event reports for product code NZX
Creator: 510(k) Report

NZXClass II21 CFR 880.5200510(k) required0 decisions0 recalls

0 FDA decisions. No recall names this code.

Enhance the performance of intravascular catheters, to maintain patency of the vascular catheter when it is not in use.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, general hospital panel

Twenty years of NZX at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FIG. 1 — NZX by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in NZX? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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